748 results · 25ms · Sources: EU EUDAMED, US FDA

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SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

LARGE CANNULATED SCREWS

FDA UDI
Smith & Nephew, Inc.·03596010063823·6.5MM UNIVERSAL CANNULATED SCREW 35MM

Cup Forceps

FDA UDI
ELLIQUENCE, LLC·00846338002398·

SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE

FDA 510(k)
FDA Class 2 ·Microbiology

IPLAN

FDA 510(k)
FDA Class 2 ·Neurology

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 12, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024

BIPAP A40

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 9, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 6, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 13, 2024

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·May 21, 2013

INTERMATE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·September 26, 2014

ALTRX +4 NEUT 44IDX62OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 2, 2011

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 16, 2024

BIPAP A40 PRO, IT

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 5, 2025

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 5, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 6, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 5, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024